Hereditäres kolorektales Karzinom: effiziente Primärprävention
Genetically defined hereditary colorectal cancer affects mostly young patients and their families and accounts for approximately 3-5% of all colorectal cancers. Early detection and clinical management determine the prognosis and are the responsibility of clinicians. While the classical variant of fa...
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| Main Authors: | , , |
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| Format: | Article (Journal) |
| Language: | German |
| Published: |
2012
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| In: |
Der Onkologe
Year: 2011, Volume: 18, Issue: 3, Pages: 207-215 |
| ISSN: | 1433-0415 |
| DOI: | 10.1007/s00761-011-2090-0 |
| Online Access: | Verlag, Volltext: http://dx.doi.org/10.1007/s00761-011-2090-0 Verlag, Volltext: https://link.springer.com/article/10.1007/s00761-011-2090-0 
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| Author Notes: | M. Kadmon, M. Kloor, M. Tariverdian |
| Summary: | Genetically defined hereditary colorectal cancer affects mostly young patients and their families and accounts for approximately 3-5% of all colorectal cancers. Early detection and clinical management determine the prognosis and are the responsibility of clinicians. While the classical variant of familial adenomatous polyposis (FAP) is characterized by a distinct phenotype, Lynch syndrome, attenuated FAP (aFAP) and MUTYH-associated adenomatous polyposis (MAP) show phenotypic overlaps which render unequivocal classification difficult. The present article elucidates the clinical manifestations, current surveillance concepts and preventive operative strategies in patients with hereditary tumor predisposition syndromes and their families. |
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| Item Description: | Gesehen am 07.08.2018 Published online first: 06 July 2011 |
| Physical Description: | Online Resource |
| ISSN: | 1433-0415 |
| DOI: | 10.1007/s00761-011-2090-0 |